- Regulatory Affairs, Senior Manager, Oncology – EU
I am currently recruiting for a Manager within Regulatory Affairs to cover the Oncology portfolio across the EU region. This company have recently acquired a strong Oncological portfolio and will soon begin several new clinical development programs within the area, therefore they are looking for a strong Regulatory Affairs professional to join the team.
- PW 6429 Manager Regulatory Affairs- Immunology
This is an excellent opportunity for an experienced regulatory professional to join our top global pharmaceutical client’s team working specifically on their Immunology portfolio. You will be responsible for Phase II / III projects, ultimately resulting in MAA preparation and filing. This company offers fantastic career development opportunities and exposure to an exciting product portfolio.
- Director Regulatory Affairs – lead early stage projects for development US, Europe and International – FULL RELOCATION to the Netherlands
Director Regulatory Affairs – lead early stage projects for development in the US, Europe and International – FULL RELOCATION to the Netherlands ... This is a Global Regulatory Lead role graded Associate Director. Please call one of Advanced Regulatory’s Principals for Regulatory Affairs, Matt Greig or Theo Moore on +44 (0)207 801 3380 or +44 (0)7918 679 405.
- Regulatory Affairs Associate Director – Operate as the GRL for Oncology
This is a highly visible position in a regulatory department that employers some of the best Netherlands regulatory professionals and deals with a number of large scale innovative research based pharmaceutical and Biotechnology projects. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore on Matt Greig on +44 (0)207 801 3380
- Senior Regulatory Program Manager
The Program Manager position will be responsible for regional (EU, ROW) regulatory strategic and operational management of a project, , or a portfolio of projects
Primary Responsibilities and Accountabilities
Is responsible for and leads the development and implementation of regional regulatory strategies on projects
Gives regional strategic regulatory input to the RAFT and Project Teams for lifecycle management of products
Analyzes regulatory environment for impact on project/p ...
- Regulatory Affairs, Oncology Europe - UK Based
I am currently partnering with an innovative, medium-sized company within the biopharmaceutical arena. This company are recruiting for a new position within their European Regulatory Affairs team due to the large amount of new clinical development programs they are running within Oncology. This role is offered at ‘Manager’ level and will cover the European region for Oncology.
- Regulatory Affairs Senior Manager – London - New and exciting regulatory affairs role for an Expanding Global Pharma company
This organisation is one that I’m sure will be able to present you with the next steps in your regulatory career – but they do want RA professional who are motivated and ready to learn. If you wish to apply for this role send your CV with a covering note to email@example.com or alternatively to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380
- Regulatory Affairs Director – Central (West) London – Regulatory Liaison & Strategy Director for Oncology
Take the lead for Oncology NME’s (Strategy, Scientific advice & Agency liaison) for an organisation that will offer your career a real boost….!!!If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380
- Regulatory Affairs Director (GRL) for Oncology Franchise - Based in Central (West) London – Medium Sized Pharma with strong Pipeline
Take strategic ownership of an early phase development portfolio for NME’s in both Oncology and CNS & Have a big impact on a developing regulatory department, where you can lead and mentor a number of talented and motivated regulatory professionals...!!! If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -
- PW 6346 European Study Manager – Oncology
An excellent opportunity for an experienced Lead CRA/ Associate Study Manager, with EU monitoring or trial management experience to join a leading Oncology biotech. You will be responsible for the management and co-ordination of EU trials with full oversight of required vendors. This is a pivotal role within an organisation who has received global recognition for their diverse portfolio. The role will start early in January, interviews to take place October.